Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.139873931_139873942delinsCAATAGATAACT , CM000666.2:g.139873931_139873942delinsCAATAGATAACT | GRCh38 |
| NC_000004.11:g.140795085_140795096delinsCAATAGATAACT , CM000666.1:g.140795085_140795096delinsCAATAGATAACT | GRCh37 |
| NC_000004.10:g.141014535_141014546delinsCAATAGATAACT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502696.1:c.111-143275_111-143264delinsAGTTATCTATTG | ||
| ENST00000509479.6:c.2079+15415_2079+15426delinsAGTTATCTATTG MANE Select | ENSP00000421180.1:n.2079+15415_2079+15426delinsAGTTATCTATTG | |
| NM_018717.4:c.2067+15415_2067+15426delinsAGTTATCTATTG | NP_061187.2:n.2067+15415_2067+15426delinsAGTTATCTATTG | |
| NM_018717.5:c.2079+15415_2079+15426delinsAGTTATCTATTG MANE Select | NP_061187.3:n.2079+15415_2079+15426delinsAGTTATCTATTG |